Canonical Allele Identifier: CA2575070237

Gene: AICDA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8605151_8605154del , CM000674.2:g.8605151_8605154del	GRCh38
NC_000012.11:g.8757747_8757750del , CM000674.1:g.8757747_8757750del	GRCh37
NC_000012.10:g.8649014_8649017del	NCBI36
NG_011588.1:g.12699_12702del , LRG_17:g.12699_12702del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.427+67_427+70del	ENSP00000445691.1:n.427+67_427+70del
ENST00000543081.6:c.427+67_427+70del	ENSP00000439103.2:n.427+67_427+70del
ENST00000544516.6:c.157-811_157-808del	ENSP00000439538.2:n.157-811_157-808del
ENST00000545576.2:n.603_606del
ENST00000696246.1:c.412+67_412+70del	ENSP00000512504.1:n.412+67_412+70del
ENST00000696271.1:n.614_617del
ENST00000696272.1:c.412+67_412+70del	ENSP00000512515.1:n.412+67_412+70del
ENST00000696273.1:c.460+67_460+70del	ENSP00000512516.1:n.460+67_460+70del
ENST00000229335.11:c.427+67_427+70del MANE Select	ENSP00000229335.6:n.427+67_427+70del
ENST00000229335.10:c.427+67_427+70del	ENSP00000229335.6:n.427+67_427+70del
ENST00000537228.5:c.427+67_427+70del	ENSP00000445691.1:n.427+67_427+70del
ENST00000543081.5:c.423+67_423+70del
ENST00000544516.5:c.153-811_153-808del
ENST00000545512.1:c.423+67_423+70del
ENST00000545576.1:n.528_531del
NM_020661.2:c.427+67_427+70del , LRG_17t1:c.427+67_427+70del	NP_065712.1:n.427+67_427+70del
XM_011520772.1:c.427+67_427+70del	XP_011519074.1:n.427+67_427+70del
XM_011520773.1:c.427+67_427+70del	XP_011519075.1:n.427+67_427+70del
NM_001330343.1:c.427+67_427+70del	NP_001317272.1:n.427+67_427+70del
NM_020661.3:c.427+67_427+70del	NP_065712.1:n.427+67_427+70del
XM_011520773.2:c.427+67_427+70del	XP_011519075.1:n.427+67_427+70del
NM_020661.4:c.427+67_427+70del MANE Select	NP_065712.1:n.427+67_427+70del
NM_001330343.2:c.427+67_427+70del	NP_001317272.1:n.427+67_427+70del